3-(Bromomethyl)-5-methylisoxazole → 2-Isopropyl-6-methoxy-1-((5-methylisoxazol-3-yl)methyl)-1H-indole-3-carbaldehyde
Reaction equation
[CH:1]([C:4]1[NH:5][C:6]2[C:11]([C:12]=1[CH:13]=[O:14])=[CH:10][CH:9]=[C:8]([O:15][CH3:16])[CH:7]=2)([CH3:3])[CH3:2].Br[CH2:18][C:19]1[CH:23]=[C:22]([CH3:24])[O:21][N:20]=1>>[CH:1]([C:4]1[N:5]([CH2:18][C:19]2[CH:23]=[C:22]([CH3:24])[O:21][N:20]=2)[C:6]2[C:11]([C:12]=1[CH:13]=[O:14])=[CH:10][CH:9]=[C:8]([O:15][CH3:16])[CH:7]=2)([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared from 2-isopropyl-6-methoxy-1H-indole-3-carbaldehyde (Compound 137) and 3-(bromomethyl)-5-methylisoxazole by General Procedure J.
Sources & evidence
- ORD record
- ord-d85cc53b90e44e3bb0e90dbb21ff1e9b
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524917B2
Reaction notes
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